A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909597



Internal ID22684807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94626109..94627584hg38UCSC Ensembl
chr8:95638337..95639812hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909597
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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